Canonical Allele Identifier: PA2827774000
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Phe1248Ser
CA285448
NM_001353952.2:c.3743T>C